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\n Related: <\/span>Fall 2025 TV Schedule: See When Your Favorite Shows Will Air<\/span><\/a>
\n\t\t<\/h3>\n<\/p><\/div>\n\n\t\t\tThe fall 2025 TV schedule is stacked \u2014 but when is your favorite show coming back? Fans of CBS\u2019 Blue Bloods are looking forward to Donnie Wahlberg\u2019s Boston Blue spinoff. Blue Bloods found a strong fan base when it premiered on CBS in 2010. After a 14-season run, viewers were not ready to say goodbye [\u2026]\t\t<\/p>\n<\/div>\n
Porter continued: \u201cI actually knew Hooters. I went to high school in college in Florida, which is where it\u2019s from. There are stadiums named for that restaurant chain and we used to do our fantasy football drafts there. But when the word scantily clad came to mind, I started thinking about lingerie. Then the word association took me to laundry, which took me to French Laundry. That is a Michelin star restaurant \u2014 and definitely not a trashy wing place. That one just made me giggle and is the one that most people are going to be laughing the most at.\u201d<\/p>\n
Despite the occasional wrong answer, Porter was proud to see his approach<\/a> work out when the $50,000 prize went to his charity.<\/p>\n\u201cThis was a win-win situation. I\u2019m a competitor, I love games and I\u2019ve watched the Weakest Link. When they tell you that you can play for a charity of your choosing, it makes it even more meaningful. The cause I chose to play for is the Huntington\u2019s Disease Society of America, which helps support families who are battling Huntington\u2019s and helps to try and find a cure for this awful disease,\u201d he told Us. \u201cI\u2019ve been a part of raising millions of dollars for research and for supporting families who are battling it. The reason it\u2019s so personal to me is my mother-in-law and my wife [Kelsey Mayfield] are both positive for Huntington\u2019s.\u201d<\/p>\n
Porter has spent years raising awareness and money<\/a> for a cure.<\/p>\n\n\n\nThank You!<\/h3>\n
You have successfully subscribed.<\/p>\n<\/p><\/div>\n<\/div><\/div>\n
\u201cMy mother-in-law is symptomatic and my wife is what they call gene positive, which means the disease will be a part of our future unless we find a cure for it. So now \u2014 more than ever \u2014 after some announcements a couple of weeks ago, we\u2019ve had some very, very promising and hopeful success within some trials in a way to limit the Huntington gene,\u201d he added. \u201cIt\u2019s just more important than ever to raise awareness, and raise money. When you go on a show like this, you\u2019re not guaranteed to win but you are guaranteed to hopefully raise awareness of what Huntington\u2019s actually is. It was something that was very meaningful to me and to go and compete made it even sweeter.\u201d<\/p>\n
For more information on Huntington\u2019s disease \u2014 including ways to support and donate \u2014 head to hdsa.org<\/a>.<\/p>\n
\u201cThis was a win-win situation. I\u2019m a competitor, I love games and I\u2019ve watched the Weakest Link. When they tell you that you can play for a charity of your choosing, it makes it even more meaningful. The cause I chose to play for is the Huntington\u2019s Disease Society of America, which helps support families who are battling Huntington\u2019s and helps to try and find a cure for this awful disease,\u201d he told Us. \u201cI\u2019ve been a part of raising millions of dollars for research and for supporting families who are battling it. The reason it\u2019s so personal to me is my mother-in-law and my wife [Kelsey Mayfield] are both positive for Huntington\u2019s.\u201d<\/p>\n
Porter has spent years raising awareness and money<\/a> for a cure.<\/p>\n You have successfully subscribed.<\/p>\n<\/p><\/div>\n<\/div><\/div>\n \u201cMy mother-in-law is symptomatic and my wife is what they call gene positive, which means the disease will be a part of our future unless we find a cure for it. So now \u2014 more than ever \u2014 after some announcements a couple of weeks ago, we\u2019ve had some very, very promising and hopeful success within some trials in a way to limit the Huntington gene,\u201d he added. \u201cIt\u2019s just more important than ever to raise awareness, and raise money. When you go on a show like this, you\u2019re not guaranteed to win but you are guaranteed to hopefully raise awareness of what Huntington\u2019s actually is. It was something that was very meaningful to me and to go and compete made it even sweeter.\u201d<\/p>\n For more information on Huntington\u2019s disease \u2014 including ways to support and donate \u2014 head to hdsa.org<\/a>.<\/p>\nThank You!<\/h3>\n